Canonical Allele Identifier: CA3352895

Gene: ERAP2 ERAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96886656T>C , CM000667.2:g.96886656T>C	GRCh38
NC_000005.9:g.96222360T>C , CM000667.1:g.96222360T>C	GRCh37
NC_000005.8:g.96248116T>C	NCBI36
NG_027839.2:g.54328A>G
NG_051092.1:g.15718T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.716T>C (ERAP2)	ENSP00000421175.2:p.Val239Ala
ENST00000437043.8:c.716T>C (ERAP2) MANE Select	ENSP00000400376.3:p.Val239Ala
ENST00000379904.8:c.715-2529T>C (ERAP2)	ENSP00000369235.4:n.715-2529T>C
ENST00000437043.7:c.716T>C (ERAP2)	ENSP00000400376.3:p.Val239Ala
ENST00000510309.1:c.716T>C (ERAP2)	ENSP00000425758.1:p.Val239Ala
ENST00000510373.5:c.716T>C (ERAP2)	ENSP00000421175.1:p.Val239Ala
ENST00000513084.5:c.716T>C (ERAP2)	ENSP00000421849.1:p.Val239Ala
NM_001130140.1:c.716T>C (ERAP2)	NP_001123612.1:p.Val239Ala
NM_022350.3:c.716T>C (ERAP2)	NP_071745.1:p.Val239Ala
XM_011543480.1:c.-705-12984A>G (ERAP1)	XP_011541782.1:n.-705-12984A>G
XM_011543481.1:c.-702-12984A>G (ERAP1)	XP_011541783.1:n.-702-12984A>G
XM_011543482.1:c.-709-12984A>G (ERAP1)	XP_011541784.1:n.-709-12984A>G
XM_011543483.1:c.-872-12984A>G (ERAP1)	XP_011541785.1:n.-872-12984A>G
XM_011543484.1:c.-701-12984A>G (ERAP1)	XP_011541786.1:n.-701-12984A>G
XM_011543485.1:c.-521-12984A>G (ERAP1)	XP_011541787.1:n.-521-12984A>G
XM_011543486.1:c.-705-12984A>G (ERAP1)	XP_011541788.1:n.-705-12984A>G
XM_011543487.1:c.-705-12984A>G (ERAP1)	XP_011541789.1:n.-705-12984A>G
XM_011543544.1:c.716T>C (ERAP2)	XP_011541846.1:p.Val239Ala
XR_948283.1:n.899T>C (ERAP2)
NM_001130140.2:c.716T>C (ERAP2)	NP_001123612.1:p.Val239Ala
NM_001329229.1:c.715-2529T>C (ERAP2)	NP_001316158.1:n.715-2529T>C
NM_001329233.1:c.716T>C (ERAP2)	NP_001316162.1:p.Val239Ala
NM_022350.4:c.716T>C (ERAP2)	NP_071745.1:p.Val239Ala
NR_137637.1:n.1427T>C (ERAP2)
XM_011543480.2:c.-705-12984A>G (ERAP1)	XP_011541782.1:n.-705-12984A>G
XM_011543481.2:c.-702-12984A>G (ERAP1)	XP_011541783.1:n.-702-12984A>G
XM_011543484.2:c.-701-12984A>G (ERAP1)	XP_011541786.1:n.-701-12984A>G
XM_011543485.2:c.-521-12984A>G (ERAP1)	XP_011541787.1:n.-521-12984A>G
XM_011543486.3:c.-705-12984A>G (ERAP1)	XP_011541788.1:n.-705-12984A>G
XM_011543544.2:c.716T>C (ERAP2)	XP_011541846.1:p.Val239Ala
XM_017009581.1:c.-547-13278A>G (ERAP1)	XP_016865070.1:n.-547-13278A>G
XM_024446113.1:c.-544-13278A>G (ERAP1)	XP_024301881.1:n.-544-13278A>G
XR_001742179.2:n.884T>C (ERAP2)
NM_022350.5:c.716T>C (ERAP2) MANE Select	NP_071745.1:p.Val239Ala